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3.
Ann Oncol ; 23(9): 2386-2390, 2012 Sep.
Article in English | MEDLINE | ID: mdl-22422944

ABSTRACT

BACKGROUND: To evaluate the efficacy of extracorporeal photopheresis (ECP) in noncutaneous T-cell lymphoma and large granular lymphocytes leukemia (LGL). PATIENTS AND METHODS: We have treated 12 refractory/relapsed patients. Six peripheral T-cell lymphoma (PTCL), one T-lymphoblastic lymphoma and five LGL with blood involvement received six biweekly leukapheresis as induction phase, followed by one course a week for 4 weeks as consolidation and one course of maintenance per month for responders until progression/relapse or disappearance of the peripheral clone. RESULTS: Six patients responded to phototherapy. Two PTCL and two LGL achieved a complete response (CR) and two other PTCL a partial response. The median duration of CR was 117 months (45-150 months) for these four patients. The peripheral clone followed by flow cytometry decreased in all six responders. Two patients with a complete disappearance of the peripheral clone have not relapsed. CONCLUSIONS: As for cutaneous T-cell lymphoma, ECP therefore to be efficient for PTCL and LGL. Early decrease and disappearance of the peripheral clone were the indicators of clinical response and nonrelapse, respectively.


Subject(s)
Leukemia, Large Granular Lymphocytic/drug therapy , Lymphoma, T-Cell/drug therapy , Photopheresis , Adult , Aged, 80 and over , Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Female , Humans , Male , Middle Aged , Treatment Outcome
4.
Biol Blood Marrow Transplant ; 18(2): 250-6, 2012 Feb.
Article in English | MEDLINE | ID: mdl-21745455

ABSTRACT

The purpose of this paper is to describe the outcome of patients who underwent double allogeneic hematopoietic stem cell transplantation (AHSCT) with reduced-intensity conditioning regimens (RIC). Forty-five patients who received double RIC-AHSCT between 1997 and 2006 were retrospectively studied. The predominant diagnosis was acute myeloid leukemia (AML) (n = 17). Other diagnoses were aplasic anemia (AA) (n = 5), myelodysplasic disorder (n = 5), acute lymphoblastic leukemia (ALL) (n = 4), chronic myelomonocytic leukemia (CML) (n = 3), myeloma (n = 3), non-Hodgkin lymphoma (NHL) (n = 3), chronic lymphocytic leukemia (CLL) (n = 2), Hodgkin's disease (HD) (n = 2), and chronic myelomonocytic leukemia (n = 1). Main indications for RIC-AHSCT 2 were relapse (n = 25, 56%) and early (n = 8, 18%) or late (n = 12, 26%) graft failure. Median delays to reach a neutrophil count of 0.5 × 10(9)/L and platelet counts of 50 × 10(9)/L were significantly smaller after the second AHSCT. Among 25 patients who relapsed after RIC-AHSCT 1, 14 patients (56%) presented a response improvement after RIC-AHSCT 2. In this group, 9 patients sustained a complete response and 5 patients a partial response. Moreover, among the 20 patients who had early or late graft failure following RIC-AHSCT 1, 9 (45%) finally reached an engraftment. Disease-free survival (DFS) was significantly improved after RIC-AHSCT 2. Thirteen patients (28%) died of transplant-related mortality (TRM) at a median delay of 69 days (range: 0-451) after RIC-AHSCT 2. Double RIC-AHSCT is a feasible procedure that allows a response or engraftment not observed after RIC-AHSCT 1. The main indication is relapse. However, TRM remains high.


Subject(s)
Hematologic Neoplasms/mortality , Hematologic Neoplasms/therapy , Hematopoietic Stem Cell Transplantation , Adolescent , Adult , Aged , Disease-Free Survival , Female , Graft Rejection/blood , Graft Rejection/mortality , Graft Survival , Hematologic Neoplasms/blood , Humans , Leukocyte Count , Male , Middle Aged , Platelet Count , Retrospective Studies , Survival Rate , Time Factors , Transplantation, Homologous
5.
Clin Microbiol Infect ; 17(9): 1387-90, 2011 Sep.
Article in English | MEDLINE | ID: mdl-21745256

ABSTRACT

The daily number of outdoor spores was counted and the cases of community-acquired invasive aspergillosis (IA) were observed over a period of 31 months. The outdoor fungal load preceding IA occurrences was significantly higher than that measured during IA-free periods, underlining the importance of preventive measures to protect high-risk patients, even at home.


Subject(s)
Air Microbiology , Aspergillosis/microbiology , Community-Acquired Infections/microbiology , Cross Infection/microbiology , Aspergillosis/transmission , Colony Count, Microbial , Community-Acquired Infections/transmission , Cross Infection/transmission , Humans , Incidence , Prospective Studies , Spores, Fungal
6.
Leukemia ; 21(9): 2020-4, 2007 Sep.
Article in English | MEDLINE | ID: mdl-17625611

ABSTRACT

One hundred de novo multiple myeloma patients with t(4;14) treated with double intensive therapy according to IFM99 protocols were retrospectively analyzed. The median overall survival (OS) and event-free survival (EFS) were 41.4 and 21 months, respectively, as compared to 65 and 37 for patients included in the IFM99 trials without t(4;14) (P<10(-7)). We identified a subgroup of patients presenting at diagnosis with both low beta(2)-microglobulin <4 mg/l and high hemoglobin (Hb) >/=10 g/l (46% of the cases) with a median OS of 54.6 months and a median EFS of 26 months, respectively, which benefits from high-dose therapy (HDT); conversely patients with one or both adverse prognostic factor (high beta(2)-microglobulin and/or low Hb) had a poor outcome. The achievement of either complete response or very good partial response after HDT was also a powerful independent prognostic factor for both OS and EFS.


Subject(s)
Antineoplastic Combined Chemotherapy Protocols/administration & dosage , Genetic Heterogeneity , Multiple Myeloma/drug therapy , Multiple Myeloma/genetics , Translocation, Genetic , Adult , Aged , Chromosomes, Human, Pair 14 , Chromosomes, Human, Pair 4 , Cytarabine/administration & dosage , Dexamethasone/administration & dosage , Disease-Free Survival , Female , Follow-Up Studies , Hemoglobins , Humans , Male , Middle Aged , Multiple Myeloma/mortality , Multivariate Analysis , Prognosis , Retrospective Studies , Vincristine/administration & dosage , beta 2-Microglobulin/blood
7.
Mycoses ; 49(5): 421-5, 2006 Sep.
Article in English | MEDLINE | ID: mdl-16922796

ABSTRACT

Since 1992, we have established a protocol of food management (restrictive diet, food distribution protocol and fungal surveillance) for allogeneic stem-cell transplant (SCT) recipients hospitalised in protected ward. This study analyses the results of 10-year surveillance of fungal contamination of this diet. Among the 456 types of foods tested filamentous fungi were isolated in 37 of them (8.1%). Aspergillus fumigatus was isolated in one type of food only, while the majority of the food was contaminated to a lower extent.


Subject(s)
Food Microbiology , Hospital Units , Program Evaluation , Aspergillus/isolation & purification , Food Service, Hospital , Germany , Humans , Mycoses/prevention & control , Retrospective Studies
8.
Leukemia ; 20(9): 1526-32, 2006 Sep.
Article in English | MEDLINE | ID: mdl-16838024

ABSTRACT

Acute lymphoblastic leukemia (ALL) in the elderly is characterized by its ominous prognosis. On the other hand, imatinib has demonstrated remarkable, although transient, activity in relapsed and refractory Philadelphia-positive acute lymphoblastic leukemia (Ph+ ALL), which prompted us to assess the use of imatinib in previously untreated elderly patients. ALL patients aged 55 years or older were given steroids during 1 week. Ph+ve cases were then offered a chemotherapy-based induction followed by a consolidation phase with imatinib and steroids during 2 months. Patients in complete response (CR) after consolidation were given 10 maintenance blocks of alternating chemotherapy, including two additional 2-month blocks of imatinib. Thirty patients were included in this study and are compared with 21 historical controls. Out of 29 assessable patients, 21 (72%, confidence interval (CI): 53-87%) were in CR after induction chemotherapy vs 6/21 (29%, CI: 11-52%) in controls (P=0.003). Five additional CRs were obtained after salvage with imatinib and four after salvage with additional chemotherapy in the control group. Overall survival (OS) is 66% at 1 year vs 43% in the control group (P=0.005). The 1-year relapse-free survival is 58 vs 11% (P=0.0003). The use of imatinib in elderly patients with Ph+ ALL is very likely to improve outcome, including OS.


Subject(s)
Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Methylprednisolone/therapeutic use , Philadelphia Chromosome , Piperazines/therapeutic use , Precursor Cell Lymphoblastic Leukemia-Lymphoma/surgery , Pyrimidines/therapeutic use , Treatment Outcome , Aged , Antineoplastic Combined Chemotherapy Protocols/administration & dosage , Antineoplastic Combined Chemotherapy Protocols/adverse effects , Benzamides , Disease-Free Survival , Humans , Imatinib Mesylate , Methylprednisolone/administration & dosage , Piperazines/administration & dosage , Pyrimidines/administration & dosage , Stem Cell Transplantation
9.
J Hosp Infect ; 62(1): 22-8, 2006 Jan.
Article in English | MEDLINE | ID: mdl-16257084

ABSTRACT

A multidisciplinary working group devoted to epidemiological surveillance of invasive aspergillosis (IA) was created in January 2000 in Grenoble University Hospital. This article presents the results of a three-year IA surveillance. The multidisciplinary working group surveyed all hospitalized patients, and the mycology laboratory detected most suspected IA cases. Cases were reviewed monthly by the Aspergillosis Committee, and were classified according to international consensus criteria. Possible nosocomial acquisition was determined. Among the 490 alerts, 74 IA cases were observed: six proven cases (8%), 36 (49%) probable cases and 32 (43%) possible cases. The incidence was 4.4 (95% CI 3.4-5.4) IA/100 000 patient-days. Among the proven and probable IA cases, we observed 10 nosocomial cases and six cases of undetermined origin. No cases were noted in the protected rooms in the haematology unit. Only one cluster of cases (three nosocomial cases) was detected in the haematology unit. Forty-three percent of cases (N=32) were hospitalized in the haematology unit, and all other cases were hospitalized elsewhere. This three-year survey found a high rate of non-nosocomial IA cases and a high frequency of IA cases hospitalized in units other than haematology. Thus, this study shows the importance of IA surveillance in haematology units and all high-risk units.


Subject(s)
Aspergillosis/epidemiology , Aspergillus/isolation & purification , Cross Infection/epidemiology , Hospitals, Teaching , Population Surveillance/methods , Aspergillosis/microbiology , Aspergillus/classification , Cross Infection/microbiology , Female , France/epidemiology , Hematologic Diseases , Hospital Units , Humans , Incidence , Male , Middle Aged , Seasons
11.
Bone Marrow Transplant ; 35(2): 165-9, 2005 Jan.
Article in English | MEDLINE | ID: mdl-15531895

ABSTRACT

Thalidomide is effective in multiple myeloma (MM), even in patients who have relapsed after high-dose therapy. A potent graft-versus-myeloma (GVM) effect can be induced against MM after allogeneic stem cell transplantation (allo-SCT). In all, 31 MM patients received thalidomide as a salvage therapy after progression following allo-SCT. The median maximum daily dose of thalidomide was 200 mg (range, 50-600). Thalidomide had to be discontinued in six patients (19%) because of toxicity. In all, nine patients (29%; 95% CI, 13-45) achieved an objective response with thalidomide therapy (six partial and three very good partial responses, VGPR). Five patients developed graft-versus-host disease (GVHD) after thalidomide therapy, including the three patients achieving a VGPR. These data demonstrate that thalidomide is potentially effective in MM patients failing allo-SCT.


Subject(s)
Hematopoietic Stem Cell Transplantation/methods , Multiple Myeloma/therapy , Salvage Therapy/methods , Thalidomide/therapeutic use , Adult , Female , Graft vs Host Disease , Hematopoietic Stem Cell Transplantation/mortality , Humans , Male , Middle Aged , Multiple Myeloma/mortality , Remission Induction , Retrospective Studies , Survival Analysis , Thalidomide/administration & dosage , Thalidomide/toxicity , Transplantation, Homologous , Treatment Outcome
13.
Bone Marrow Transplant ; 32(10): 993-9, 2003 Nov.
Article in English | MEDLINE | ID: mdl-14595387

ABSTRACT

To determine the results of allogeneic hematopoietic stem cell (HSC) transplantation for chronic myelogenous leukemia (CML) at various stages of the disease in children, a retrospective analysis was carried out on the outcome of transplants performed on 76 children and teenagers with CML between 1982 and 1998. In all, 60 patients were transplanted from a matched sibling donor (MSD) and 16 from a matched unrelated donor (MUD). There was a higher incidence of acute graft-versus-host disease after MUD transplantation (P<10(-3)). The main cause of death was transplant-related toxicity in both groups. In MSD recipients, the probability of relapse at 5 years for patients transplanted in the first chronic phase was lower than in patients transplanted in the advanced phase (relative risk (rr)=5.90; 95% confidence interval (CI), 1.85-18.82, P<0.01). The estimated 5-year event-free survival (EFS) rate was higher after MSD vs MUD transplantation (61% (95% CI, 48-73%) vs 27% (95% CI, 4-49%), rr=0.25, P<10(-3)). In children transplanted from MSD, the 5-year EFS was higher when transplantation was performed in the first chronic phase vs the advanced phases (73% (95% CI, 59-87%) vs 32% (95% CI, 10-54%), P<10(-3)). Disease status at transplantation was the unique factor influencing survival in patients undergoing transplantation from MSD with a better outcome for those transplanted in the first chronic phase. Allogeneic HSC offers a possibility of curing childhood CML with a significant advantage for patients transplanted in chronic phase using a human leukocyte antigen-identical sibling donor.


Subject(s)
Leukemia, Myelogenous, Chronic, BCR-ABL Positive/therapy , Adolescent , Bone Marrow Transplantation/mortality , Child , Child, Preschool , Disease Progression , Female , Graft vs Host Disease/etiology , Humans , Leukemia, Myelogenous, Chronic, BCR-ABL Positive/mortality , Male , Retrospective Studies , Risk Factors , Survival Analysis , Tissue Donors , Transplantation, Homologous , Treatment Outcome
14.
J Clin Oncol ; 19(14): 3340-9, 2001 Jul 15.
Article in English | MEDLINE | ID: mdl-11454881

ABSTRACT

PURPOSE: To analyze the impact of pre- and posttransplantation factors on the outcome of allogeneic transplantation after nonmyeloablative conditioning regimens. PATIENTS AND METHODS: Ninety-two allogeneic transplantations after nonmyeloablative preparative regimens were reported to the Société Française de Greffe de Moelle Registry registry. Initial diagnoses were lymphoid diseases (n = 22), myeloma (n = 14), acute leukemia and myelodysplasia (n = 41), chronic myelogenous leukemia (n = 12), and solid tumors (n = 3). Forty-six patients had previously received a transplant, and 49 had progressive disease before transplantation. Three types of conditioning regimens were used with fludarabine or antithymocyte globulins. Eighty-nine patients underwent transplantation, 60 from peripheral-blood progenitor cells. Eighty-six patients received graft-versus-host disease (GHVD) prophylaxis for a median duration of 53 days. RESULTS: Seventy-nine patients engrafted, with 40 complete and 21 mixed chimerisms. The acute GHVD rate at 3 months was 50% +/- 11%. Fifty-two patients achieved complete remission and 12, partial remission. At 18 months after transplantation, the overall survival (OS) and the transplant-related mortality (TRM) were 32% +/- 12% and 38% +/- 14%, respectively. Initial diagnosis and disease status before transplantation significantly influenced survival. Age and GHVD prophylaxis type significantly influenced TRM. We also showed an impact of GHVD prophylaxis duration on OS and TRM. In multivariate analysis, three factors remained of prognostic value on OS: initial diagnosis, disease status at transplantation, and GHVD prophylaxis duration. CONCLUSION: This series shows encouraging results from nonmyeloablative conditioning regimens before allotransplantation and demonstrates the impact of some pre- and posttransplantation factors on outcome after transplantation.


Subject(s)
Hematopoietic Stem Cell Transplantation , Transplantation Conditioning , Adolescent , Adult , Child , Female , Graft vs Host Disease , Humans , Male , Middle Aged , Multivariate Analysis , Neoplasms/therapy , Remission Induction , Retrospective Studies , Survival Analysis , Transplantation, Homologous , Treatment Outcome
15.
Leukemia ; 15(4): 642-6, 2001 Apr.
Article in English | MEDLINE | ID: mdl-11368368

ABSTRACT

Non-myeloablative allogeneic stem cell transplantation has been reported to induce sustained complete remission even in advanced diseases (acute leukemia, lymphomas). The tolerance of this procedure allows treatment of poor candidates to conventional allogeneic transplantation with persisting or relapsing myeloma patients. Twelve patients previously treated with at least VAD regimen and autologous transplantation were included. All patients had a serum beta2 microglobuline >3 mg/l at diagnosis. The conditioning regimen consisted of fludarabine 25 mg/m/day x 5, antithymoglobulin 2.5 mg/kg/day x 5, busulphan 2 mg/kg/day x 2; the transplant was peripheral stem cells (except one) from an HLA-matched sibling and was followed by cyclosporin for 45 to 90 days. This treatment results in a well-tolerated procedure (no mucositis, duration of aplasia <7 days). A dramatic graft anti-myeloma effect is documented even in progressive disease (11/12 PR + CR, 4/12 CR). However, five patients underwent CMV disease, one died of CMV encephalitis (UPN 3) and delayed severe GVHD occurred in four patients. Our data suggest that a better survival could be achieved when patients are transplanted with a controlled disease. In high risk patients, we now propose a non-myeloablative transplantation in addition to the conventional and intensive chemotherapy as first-line of treatment.


Subject(s)
Hematopoietic Stem Cell Transplantation , Multiple Myeloma/therapy , Graft vs Host Disease/etiology , Hematopoietic Stem Cell Transplantation/adverse effects , Humans , Middle Aged , Multiple Myeloma/blood , Pilot Projects , Salvage Therapy , Transplantation Conditioning , Transplantation, Autologous , Transplantation, Homologous
17.
Br J Haematol ; 111(1): 292-302, 2000 Oct.
Article in English | MEDLINE | ID: mdl-11091216

ABSTRACT

In this retrospective multicentre study, we analysed the results of 82 consecutive second early allogeneic transplants for primary (n = 28) or secondary ([n = 54) graft failures performed between 1985 and 1997 in patients with acute leukaemia (n = 33), aplastic anaemia (n = 29) or chronic myeloid leukaemia (n = 20). HLA-matched siblings were used in 64 cases. The same donors were used for both transplants in 56 cases and the first transplant was T-cell depleted in 30 cases. The median age at transplant was 25 years and the median intertransplant time interval was 2 months. Estimates of the 3-year overall survival and day 100 transplant-related mortality were 30% and 53% respectively. A recipient age < 34 years at transplant, an intertransplant time interval > or = 80 d and a positive recipient cytomegalovirus serology were predictors of a better outcome. The use of cyclosporin A (CsA) after second transplant had a dramatic impact on outcome, the best results being observed with CsA alone. The day 40 probability of neutrophil recovery was 73%. The use of peripheral blood progenitor cells (PBPCs) was associated with a higher and faster neutrophil recovery. Other factors associated with neutrophil recovery were an intertransplant time interval > or = 80 d and a positive recipient cytomegalovirus serology. Therefore, second early allogeneic transplantation for graft failure is an effective treatment, especially if patients can receive CsA for graft-versus-host disease prevention and are retransplanted more than 80 d from first transplant.


Subject(s)
Graft Rejection/surgery , Hematopoietic Stem Cell Transplantation , Leukemia/surgery , Adolescent , Adult , Anemia, Aplastic/surgery , Chi-Square Distribution , Child , Child, Preschool , Cyclosporine/therapeutic use , Female , Follow-Up Studies , Graft vs Host Disease/diagnosis , Humans , Immunosuppressive Agents/therapeutic use , Infant , Leukemia, Myelogenous, Chronic, BCR-ABL Positive/surgery , Male , Middle Aged , Proportional Hazards Models , Reoperation , Retrospective Studies , Statistics, Nonparametric , Transplantation, Homologous , Treatment Outcome
18.
Leukemia ; 14(9): 1667-77, 2000 Sep.
Article in English | MEDLINE | ID: mdl-10995015

ABSTRACT

The recent clinical trial in lymphoma using tumor antigen-loaded DCs (Hsu et al, Nature Med 1996; 2: 52) demonstrates the efficiency of the use of professional antigen presenting cells (APCs) for taking up, processing and presenting tumor protein in a vaccine strategy in cancer. However, the production of large quantities of clinical grade APCs remains to be resolved. Here, we describe that both dendritic cells (DCs) and macrophages (MOs) can be efficiently differentiated in large numbers from lymphoma patients in spite of their disease and previous therapy. These cells were produced using the VAC and MAK cell processors according to standard operating procedures. DCs and MOs were differentiated from circulating monocytes in gas permeable hydrophobic bags, with 2% autologous serum and in the presence of GM-CSF and IL-13 or GM-CSF alone, respectively. DCs and MOs were then purified by counter flow centrifugation. Phenotypic, morphological and functional analysis showed that cells differentiated from patients with lymphoma present quite similar features to DCs and MOs produced from monocytes of healthy donors. Moreover, we show that MOs, when combined with CD20 antibody (Rituximab), can efficiently engulf tumor cells and propose that a such combination could be used for initiating a clinical trial in lymphoma. Thus, the possibility of producing functional DC and MOs in large amounts in conditions compatible with therapeutic application will allow the development of new immune strategies to eradicate lymphoma.


Subject(s)
Antigen-Presenting Cells , Cell Differentiation , Dendritic Cells , Lymphoma, Non-Hodgkin/therapy , Macrophages , Adult , Antigen Presentation/physiology , Female , Humans , Leukocytes, Mononuclear/pathology , Lymphocyte Activation/physiology , Lymphoma, Non-Hodgkin/pathology , Male , Middle Aged , Phagocytosis , Phenotype , Receptors, Fc/physiology , T-Lymphocytes/physiology
19.
Hematol J ; 1(4): 274-81, 2000.
Article in English | MEDLINE | ID: mdl-11920202

ABSTRACT

INTRODUCTION: Non-myeloablative peripheral stem cell transplantation has been shown to induce tumour rejection in patients with acute leukaemia. However, the immunological mechanisms involved and the immune reconstitution achieved have not been investigated. MATERIALS AND METHODS: We describe the cases of two patients for whom we have studied the lymphocyte reconstitution achieved, using both phenotypic and genetic analyses of the T-cell repertoire, after peripheral stem cell transplantation. RESULTS: : In both cases we observed immune reconstitution with T-cell repertoire evolution and presence of activated CD8(+) T cells. In one of the patients an activated clone expressing Vbeta8 represents 46% of the CD8(+) cells. Expansion of this clone occurred in the absence of graft vs host disease symptoms. In the second case a skin lesion typical of graft vs host disease appeared after complete remission had been achieved. The T-cell repertoire in a biopsy of the lesion was distinct from that observed in the blood. CONCLUSION: Our study indicates that peripheral donor cells can effectively reconstitute a grafted patient while inducing an immune response against antigens expressed by the leukaemic/myeloma cells. Our data provide arguments for different populations of T cells associated with graft vs leukaemia/lymphoma and GVH effects.


Subject(s)
Blood/immunology , Hematopoietic Stem Cell Transplantation , Immunotherapy/methods , Skin/cytology , Acute Disease , Antineoplastic Combined Chemotherapy Protocols/administration & dosage , Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Blood Cells/immunology , CD8-Positive T-Lymphocytes/cytology , CD8-Positive T-Lymphocytes/immunology , Carmustine/administration & dosage , Clone Cells/immunology , Cyclophosphamide/administration & dosage , Cytarabine/administration & dosage , Daunorubicin/administration & dosage , Dexamethasone/administration & dosage , Doxorubicin/administration & dosage , Female , Graft Survival , Graft vs Host Reaction/immunology , Graft vs Leukemia Effect/immunology , Humans , Immunophenotyping , Leukemia, Myeloid/drug therapy , Leukemia, Myeloid/therapy , Male , Middle Aged , Minisatellite Repeats , Multiple Myeloma/drug therapy , Multiple Myeloma/therapy , Prednisone/administration & dosage , Receptors, Antigen, T-Cell, alpha-beta/analysis , Skin/immunology , T-Lymphocyte Subsets/cytology , Transplantation Conditioning , Transplantation, Homologous/immunology , Vincristine/administration & dosage , Whole-Body Irradiation
20.
Eur J Immunol ; 29(10): 3188-95, 1999 10.
Article in English | MEDLINE | ID: mdl-10540330

ABSTRACT

This article describes the study of the functional relationship between auto-tumor-reactive CD4(+) T cell clones (TCC) and autologous malignant B cells. Four auto-tumor-reactive CD4(+) TCC were derived from tumor-infiltrating T lymphocytes (TIL-T) from a freshly isolated human follicular lymphoma by the following technique: total CD4(+) TIL-T were negatively purified by an immunomagnetic procedure, then CD4(+) TCC were obtained by limiting dilution in the presence of IL-2 and autologous non-irradiated follicular lymphoma cells as feeders. After expansion, these CD4(+) TCC were co-cultured with non-irradiated autologous malignant B cells. All four TCC were activated by B lymphoma cells and proliferated, as assessed by CD25 expression and cell cycle analysis. Activation and proliferation of B lymphoma cells were studied in response to activated CD4(+) T cells. Although all four TCC were able to induce B lymphoma cell activation (Ki-67 antigen induction and CD40 up-regulation), cells were subsequently blocked in G1 phase. Activation of B-NHL cells was mediated by TCR-HLA class II interaction, as shown by a blocking experiment using an anti-CD4 monoclonal antibody (mAb). Since anti-CD40 mAb with or without IL-4 did not induce proliferation of B lymphoma cells in contrast to normal B cells, we suggest that the blockade in G1 phase is due to the presence of abnormalities in B lymphoma cells. This is the first evidence that autologous reactive CD4(+) TCC can engage follicular lymphoma B cells to enter the cell cycle and induce an aborted activation stage.


Subject(s)
CD4-Positive T-Lymphocytes/immunology , Cell Communication/immunology , Lymphocyte Activation/immunology , Lymphoma, B-Cell/immunology , Antibodies, Monoclonal/pharmacology , CD40 Antigens/immunology , CD40 Ligand , Cell Cycle/immunology , Cell Division/immunology , Clone Cells , Coculture Techniques , G1 Phase/immunology , Humans , Interleukin-4/pharmacology , Ki-67 Antigen/biosynthesis , Ki-67 Antigen/immunology , Ligands , Membrane Glycoproteins/physiology
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